Triangulation mechanism for a minimally invasive surgical device

ABSTRACT

A surgical device including a seal anchor that includes leading and trailing portions. A plurality of ports longitudinally extends between the leading and trailing portions. The ports are adapted and configured to receive surgical objects therein. At least one of the surgical objects is a viewing instrument including a viewing portion. During a surgical procedure, surgical objects inserted in the other ports are selectively positionable with respect to the viewing instrument.

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a continuation of U.S. patent application Ser. No.13/483,553 filed May 30, 2012, now U.S. Pat. No. 8,845,517, which claimsbenefit of U.S. Provisional Application No. 61/501,282 filed Jun. 27,2011, and the disclosures of each of the above-identified applicationsare hereby incorporated by reference in their entirety.

BACKGROUND

Technical Field

The present disclosure relates generally to a surgical device for use ina minimally invasive surgical procedure. More particularly, the presentdisclosure relates to a surgical portal device adapted and configured toreceive surgical instruments therein, and to reposition the distal endsof the surgical instruments that are placed within the surgical portaldevice.

Background of Related Art

A minimally invasive surgical procedure is one in which a surgeon entersa patient's body through one or more small openings in the patient'sskin or a naturally occurring opening (e.g., mouth, anus, or vagina). Ascompared with traditional open surgeries, minimally invasive surgicalprocedures have several advantages and disadvantages. Minimally invasivesurgeries include arthroscopic, endoscopic, laparoscopic, and thoracicsurgeries. Advantages of minimally invasive surgical procedures overtraditional open surgeries include reduced trauma and recovery time forpatients.

However, some disadvantages include a lack of direct visualization ofthe surgical site and reduced dexterity of instruments, as compared totraditional open surgeries. In particular, the simultaneous manipulationof the viewing instrument and surgical instruments that are insertedinto the opening may be complicated. One complication arises from thedifficulty in visualizing surgical instruments on a monitor that isoperably coupled to the viewing instrument.

One surgical technique used to increase the ability of the surgeon tovisualize and access critical anatomy is triangulation. Triangulation isa principle in which the positioning of the surgical instruments may bedetermined by having known initial positions of the instruments withrespect to a given point, e.g., another device or instrument, andtracking the change in position from that initial position. One methodof triangulation involves holding the surgical instrument and theviewing instrument so that their tips form the apex of an imaginarytriangle. By knowing the initial positions of surgical instruments withrespect to a given point and by tracking the change in position, thecoordinates of the surgical instruments are determinable.

In conventional minimally invasive surgical procedures, triangulation isachieved through insertion of multiple instruments through multipleopenings. In most minimally invasive surgical procedures through asingle incision, straight and rigid surgical instruments are insertedthrough a single incision. To control the instruments, a surgeon oftencrosses his hands. The lack of triangulation makes visualization andaccess of critical anatomy potentially difficult.

Furthermore, the placement of multiple instruments through a singleincision increases the potential of interference among thoseinstruments. It would be advantageous to space those instruments apartwithin the surgical site, without necessitating a larger incision.

Consequently, a continuing need exists for improved minimally invasivesurgical devices.

SUMMARY

Disclosed herein is a surgical system for use during a minimallyinvasive surgical procedure. The surgical system includes a seal anchormember for positioning within a tissue tract accessing an underlyingbody cavity and a triangulation device including a viewing instrumentand one or more surgical instruments. The viewing instrument includes aviewing portion. The one or more surgical instruments may betriangulated with respect to the viewing portion of the viewinginstrument.

The seal anchor member defines a longitudinal axis and includes leadingand trailing ends. A plurality of ports extends longitudinally betweenthe leading and trailing ends. Each port is configured and adapted toreceive surgical instruments therethrough. A lumen is substantiallycentrally positioned along a longitudinal axis of the seal anchor and isconfigured and adapted to receive a surgical instrument therethrough,e.g., a viewing instrument including a viewing portion. In anembodiment, the lumen may receive a tube through which a viewinginstrument, e.g., an endoscope is placed. The surgical instrumentsplaced within the ports are configured and adapted to transition betweena condition in which distal portions of the surgical instruments aresubstantially parallel with respect to the longitudinal axis of theviewing instrument and a condition in which the distal portions of thesurgical instruments are angled with respect to the longitudinal axisviewing instrument. The angling of the surgical instruments with respectto the longitudinal axis of the viewing instrument facilitatestriangulation.

Embodiments of mechanisms to effect triangulation of surgicalinstruments with respect to a viewing instrument that are placed withina seal anchor member, such as that described above, are disclosedherein. In one embodiment, a tube is placed within the centrallydisposed lumen of the seal anchor. The tube is dimensioned for thereception of a viewing instrument therein. The tube includes a threadingdisposed about the distal portion of the tube. The tube is dimensionedto accommodate reception of a viewing instrument therein. A linkageoperably couples each of the surgical instruments to the tube. Inparticular, the linkage may include first and second arms that arepivotably connected to the surgical instruments and a collar that ispositioned about the tube. The tube may include threading thatcorresponds to threading on the collar such that rotation of the tubeeffects axial translation of the collar with respect to the tube. As thecollar axially translates, the linkage mechanism transitions between afirst state in which the first and second arms are angled with respectto one another and a second state in which the which the angle betweenthe first and second arms is equal to 180 degrees, i.e., the first andsecond arms are parallel (for example, the first and second arms may becoaxial). The transitioning of the linkage mechanism between the firstand second states determines the distance between the viewing instrumentand the surgical instruments and thereby determines whether the surgicalinstruments are bent or angled with respect to the longitudinal axis ofthe seal anchor member. In an embodiment, the viewing instrument, e.g.,an endoscope may be placed within a tube.

In another embodiment, a band formed from a sufficiently compliantmaterial is biased toward a first, enlarged diameter and istransitionable to a second smaller diameter. The band also has aplurality of intermediate diameters between the first and seconddiameters. The band is operably coupled to the surgical instruments. Theforce necessary to bend or angle the surgical instruments corresponds tothe position of the surgical instruments within ports of the seal anchormember. In particular, distal translation of the surgical instrumentsfacilitates transitioning of the band to the first enlarged diameter,thereby effecting bending of the surgical instruments.

In a still further embodiment, a tube includes a balloon that isradially expandable to exert a force upon surgical instruments radiallypositioned about the tube to effect angling or bending of the surgicalinstruments with respect to the tube.

These and other features of the current disclosure will be explained ingreater detail in the following detailed description of the variousembodiments.

BRIEF DESCRIPTION OF THE DRAWINGS

Various embodiments of the present disclosure are described hereinbelowwith reference to the drawings, wherein:

FIG. 1 is a front perspective view of a seal anchor member shown in anexpanded condition and positioned relative to tissue;

FIG. 2 is a top view of the seal anchor member of FIG. 1;

FIG. 3 is a cross-sectional view of the seal anchor member of FIG. 1taken along section line 3-3 illustrating a port that extendslongitudinally therethrough;

FIG. 4 is a view of the port of FIG. 3 with a surgical object insertedtherethrough;

FIG. 5 is a perspective view of the seal anchor member of FIG. 1 shownin a compressed condition and prior to the insertion thereof into anopening in tissue;

FIG. 6 is an embodiment of a triangulation device in accordance with thepresent disclosure;

FIG. 7 is a perspective view of an embodiment of a triangulation systemincluding the triangulation device of FIG. 6 shown operably coupled tothe seal anchor member of FIG. 1 and shown in a first condition;

FIG. 8 is a perspective view of the triangulation system of FIG. 7 shownin a second condition;

FIG. 9 is another embodiment of a triangulation device in accordancewith the present disclosure;

FIG. 10 is a top view of the triangulation device of FIG. 9;

FIG. 11 is a perspective view of another embodiment of a triangulationsystem including the triangulation device of FIG. 9 shown in a firstcondition;

FIG. 12 is a perspective view of the triangulation system of FIG. 11shown in a second condition;

FIG. 13 is a perspective view of another embodiment of a triangulationsystem in accordance with the present disclosure shown in a first state;and

FIG. 14 is a perspective view of the triangulation system of FIG. 13shown in a second state.

DETAILED DESCRIPTION OF THE EMBODIMENTS

Particular embodiments of the present disclosure will be describedherein with reference to the accompanying drawings. As shown in thedrawings and as described throughout the following descriptions, and asis traditional when referring to relative positioning on an object, theterm “proximal” will refer to the end of the apparatus that is closestto the clinician during use, and the term “distal” will refer to the endthat is farthest from the clinician during use.

With reference to FIGS. 1-5, a seal anchor member 100 will now bedescribed. The seal anchor member 100 is configured and adapted to beplaced within an opening “O”, e.g., an incision or naturally occurringbodily orifice, within tissue “T” defining a tissue tract for accessingan underlying body cavity. The seal anchor member 100 may form asubstantially seal with the tissue tract defined by the opening “O” toaccess an underlying body cavity while inhibiting the escape ofinsufflation gasses within the body cavity. To facilitate placement andsecurement of the seal anchor member 100 within the opening “O”, theseal anchor member 100 is transitionable between an expanded condition(FIG. 1) and a compressed condition (FIG. 5). The seal anchor member 100has an internal biasing force that biases the seal anchor member 100toward the expanded condition.

The seal anchor member 100 defines a longitudinal axis “A” and includesrespective trailing and leading sections 102, 104. An intermediatesection 106 is disposed between the trailing and leading sections 102,104. The seal anchor member 100 includes one or more ports 108 a-c thatextend longitudinally through the seal anchor member 100 and between thetrailing and leading sections 102, 104. A lumen 109 extendslongitudinally through the seal anchor member 100 and is substantiallycentrally disposed. The ports 108 a-c and the lumen 109 may have thesame or different diameters. For example, the ports 108 a-c may have thesame diameter, while the lumen 109 may have another diameter.Alternatively, the ports 108 a-c may each have a different diameter.

In the expanded condition, the seal anchor member 100 is at rest and therespective radial dimensions D₁, D₂ of the trailing and leading sections102, 104 of the seal anchor member 100, as well as radial dimension R ofthe intermediate portion 106, are such that insertion the seal anchormember 100 into the opening “O” is inhibited since the opening “O”defines a lesser radial dimension. However, in the compressed condition,trailing and leading sections 102, 104 of the seal anchor member 100, aswell as the intermediate portion 106 are dimensioned for insertion intothe opening “O”.

The seal anchor member 100 includes ports 108 a-c. A lumen 109 iscentral disposed between the ports 108 a-c. Each of the ports 108 a-cand the lumen 109 may be configured and adapted to receive surgicalobjects “I” (FIG. 3) therethrough in a substantially sealedrelationship. In particular, the lumen 109 may receive an instrument,e.g., tube 250, therein.

Although discussed with respect to port 108 c, the following isillustrative of how ports 108 a-c and lumen 109 cooperate with aninserted instrument. As shown in FIG. 3, prior to the insertion ofsurgical object “I” within port 108 c, the port 108 c defines an initialradial dimension D_(P1), which is generally about 0 mm to inhibit theescape of insufflation gas that may be present within the body cavity.For example, port 108 c may be a slit extending the longitudinal lengthof seal anchor member 100 through proximal and distal sections 104, 104.Alternatively, the port 108 c may define an opening within seal anchormember 100 having an initially open state.

Upon the introduction of surgical object “I”, port 108 c transitions toa second state in which port 108 c defines a second, larger dimensionD_(P2) that substantially approximates diameter D_(I) of surgical object“I” such that a substantially fluid-tight seal is formed therewith,thereby forming a sealed relationship between the port 108 c and thesurgical object “I”. The sealed relationship between the port 108 c andthe surgical object “I” substantially inhibiting the escape ofinsufflation gas through port 108 c of seal anchor member 100 when thesurgical object “I” is inserted therein. D_(I), and thus D_(P2), willgenerally lie within the range of about 5 mm to about 12 mm, as thesedimensions are typical of the surgical objects used during the course ofminimally invasive procedures. However, a seal anchor member 100including a port 108 a-c may exhibit substantially larger, or smallerdimensions in the second state. In an embodiment, the seal anchor member100 may be initially devoid of ports 108 a-c, and may be created duringuse through the insertion of one or more surgical objects “I” throughthe seal anchor member 100.

As depicted in FIG. 5, as seal anchor member 100 is compressed under theinfluence of external force “F”, an internal biasing force “F_(B1)” iscreated within seal anchor member 100 that is directed outwardly,opposing force “F”. Internal biasing force “F_(B1)” endeavors to expandseal anchor member 100 and thereby return seal anchor member 100 to theexpanded condition thereof. Accordingly, as long as seal anchor member100 is subject to external force “F”, seal anchor member 100 remains inthe compressed condition. Upon the removal of external force “F”,however, biasing force “F_(B1)” acts to return seal anchor member 100 tothe expanded condition. In the compressed state, the seal anchor member100 defines a reduced radial dimension. In particular, the trailingsection 102 defines a radial dimension D₁′, the leading section 104defines a radial dimension D₂′, and the intermediate section 106 definesa radial dimension R. The reduced radial dimension of the seal anchormember 100 facilitates insertion of the seal anchor member 100 into theopening “O” within tissue “T”. Subsequent to insertion, the naturalbiasing force of the seal anchor member 100 transitions the seal anchormember 100 to the initial, greater radial dimension, therebyfacilitating securing the seal anchor member 100 within the opening “O”,and inhibiting the escape of insufflation gas.

The compressible material comprising seal anchor member 100 alsofacilitates the resilient transitioning of port 108 a-c between itsfirst closed state (FIG. 3) and its second state (FIG. 4). As previouslydiscussed, prior to the insertion of surgical object “I”, port 108 a-cis in its first state in which port 108 a-c defines a first or initialdimension D_(P1). Port 108 a-c may incorporate a slit extending thelongitudinal length of seal anchor member 100. In this first state, port108 a-c is at rest and is not subject to any external forces. However,upon the introduction of surgical object “I” through port 108 a-c asdepicted in FIG. 4, the surgical object “I” exerts a force “F_(I)” uponport 108 a-c that is directed radially outward. Force “F₁” acts toenlarge the dimensions of port 108 a-c and thereby transition port 108a-c into the second state thereof in which port 108 a-c defines asecond, larger dimension D_(P2) that substantially approximates thediameter D_(I) of surgical object “I”. Consequently, an internal biasingforce “F_(B2)” is created that is directed radially inward, inopposition to force “F_(I)”. Internal biasing force “F_(B2)” endeavorsto return port 108 a-c to reduce the internal dimension of port 108 a-cand thereby return port 108 a-c to the first state thereof. Internalbiasing force “F_(B2)” is exerted upon surgical object “I” and acts tocreate a substantially fluid-tight seal therewith.

Referring again to FIG. 1, one or more positioning members 114 a-b maybe associated with either or both of trailing (or proximal) end 102 anddistal (or leading) end 104, respectively, of seal anchor member 100.Positioning members 114 a-b may be composed of any suitablebiocompatible material that is at least semi-resilient such thatpositioning members 114 a-b may be resiliently deformed and may exhibitany suitable configuration, e.g., substantially annular or oval. Priorto the insertion of seal anchor member 100, positioning members 114 aredeformed in conjunction with the respective proximal and distal ends102, 104 of seal anchor member 100 to facilitate the advancement thereofthrough tissue tract T (FIG. 5). Subsequent to the insertion of sealanchor member 100 within tissue tract T, the resilient nature ofpositioning members 114 a-b allows positioning members to return totheir normal, substantially annular configuration, thereby aiding in theexpansion of either or both of the respective proximal and distal ends102, 104 and facilitating the transition of seal anchor member 100 fromits compressed condition to its expanded condition. Positioning members114 also may engage the walls defining the body cavity to furtherfacilitate securement of seal anchor member 100 within the body tissue.For example, positioning member 114 a-b at leading end 104 may engagethe internal peritoneal wall and positioning member 114 a-b adjacenttrailing end 102 may engage the outer epidermal tissue adjacent theopening “O” within tissue “T”. In another embodiment of seal anchormember 100, one or more additional positioning members 114 a-b may beassociated with intermediate portion 106.

The seal anchor member 100 may be operably coupled to a triangulationdevice to form a triangulation system. An embodiment of a triangulationsystem including a triangulation device operably coupled to the sealanchor member 100 will now be described with reference to FIGS. 6-8. Atriangulation system 200 (FIGS. 7 and 8) includes the seal anchor member100 and a triangulation device 200A including surgical instruments 270that are configured and adapted to be received within the seal anchormember 100 and to transition between at least two configurations. In afirst configuration, at least one surgical instrument 270 may define anaxis that is substantially parallel to the longitudinal axis “A” of theseal anchor member 100. In a second configuration, the at least onesurgical instrument 270 defines an axis that is angled with respect tothe longitudinal axis “A”. It is preferable to insert or remove thetriangulation system 200 while in the first configuration due to therelative smaller diameter of the triangulation system 200 while in thefirst configuration as compared to the triangulation system 200 while inthe second configuration.

As shown best in FIG. 6, the triangulation device 200A includes at leastone surgical instrument 270 and a tube 250 including a viewing portion253 (FIG. 8). The surgical instruments 270 are receivable within theports 108 a-c. The tube 250 is receivable within the lumen 109. Thesurgical instruments 270 are radially disposed about the tube 250.

The at least one surgical instrument 270 includes an end-effector 272.The surgical instrument 270 and/or the end-effector 272 may besubstituted with a suitable instrument 270 and/or end-effector 272 asnecessitated by the particular surgical procedure. The surgicalinstrument 270 may be hinged or may be formed from a compliant materialsuch that the surgical instrument 270 may be angled with respect thelongitudinal axis “A”. In an embodiment, surgical instrument 270 mayinclude a weakened or hinged region 270 a such that application of aforce in the weakened or hinged region effects bending of the surgicalinstrument at the weakened or hinged region.

By bending the surgical instrument 270, the distal end of the surgicalinstrument and therefore the end effector 272 is inwardly translatedtoward the center of the seal anchor 100 and substantially within thefield of view of the viewing portion 253 of the viewing instrument 251.For example, the end effectors 272 of the surgical instruments 270 maybe across the path of the viewing instrument 251. As shown in FIG. 6,surgical instrument 270 may include a hinge or a weakened region 270 ato facilitate bending of the surgical instrument 270 in the desireddirection, e.g., toward the viewing portion 253 of the tube 250. Byplacing the surgical instrument 270 in the field of view of the viewingportion 253, visualization of the surgical procedure is achieved.

As shown in FIG. 6, the triangulation device 200A includes threesurgical instruments 270 that are radially spaced a distance apart fromthe centrally disposed tube 250. Moreover, as shown in FIGS. 6 and 7,the surgical instruments 270 are transitionable between a firstorientation in which the surgical instruments 270 define axes that aresubstantially parallel to one another (FIG. 7), and a second orientationin which the surgical instruments 270 define axes that are intersecting,i.e., the surgical instruments 270 are angled with respect to oneanother.

A linkage mechanism 280 operably connects the tube 250 and the surgicalinstruments 270. The linkage mechanism 280 facilitates transitioning ofthe transitioning of the triangulation system 200 between first andsecond configurations. As shown in FIGS. 7 and 8, the tube 250 may berotated about axis “A” in the direction of directional arrow “Z”. Byrotating the tube 250, the angle of the surgical instruments 270 withrespect to the longitudinal axis “A” is adjusted.

As shown in FIG. 6, the linkage mechanism 280 includes a collar 251 thatis positioned about the tube 250 and is translatable along axis “A”. Thecollar 251 includes an internal threading that corresponds to threading255 disposed about the surface of the tube. In an embodiment, a viewinginstrument may be manufactured to have threading on an exterior surfaceand may be substituted for the tube 250.

Each surgical instrument 270 may be formed from sufficiently compliantmaterial such that application of a force against the surgicalinstrument 270 results in bending of the surgical instrument 270.Operably connecting each surgical instrument 270 to each other is a band271 positioned about the surgical instrument 270. The band 271 ispivotably connected to a first arm member 281 that is pivotablyconnected to a second arm member 283. The second arm member 283 ispivotably connected to the collar 251.

In the first configuration, the first and second arm members 281, 283define a first angle α with respect to one another such that thedistance between the band 271 and the collar 251 and band 271 is a firstdistance d from one another. In the second configuration, the first andsecond arm members 281, 283 define a second angle β with respect to oneanother and the collar 251 and the band 271 is a second distance D fromone another. The first and second arm members 281, 283 defineintermediate angles between first angle α and second angle α, and thecollar 251 and the band 271 define a plurality of distances betweenfirst distance d and second distance D. The surgical instruments 270 mayalso be axially translatable through the ports 108 a-d in a synchronizedor in an independent fashion. Moreover, the bands 271 may slide alongthe surgical instruments 270 thereby facilitating axial translation ofthe surgical instrument 270 that is independent from the axialtranslation of the tube 250. The threading 255 along the tube 250 may beuniformly spaced such that rotation of the tube 250 along or againstdirectional arrow “Z” results in a predictable movement of the tubes250. By knowing the initial coordinates of each surgical instrument 270,and in particular the end effector 272 of each surgical instrument 270,tracking of the coordinates, i.e., the position, of each surgicalinstrument 270 is achieved.

Another embodiment of a triangulation system will now be described withrespect to FIGS. 9-12. Triangulation system 300 includes a triangulationdevice 300A, a tube 350 adapted to receive therein a viewing instrument251 including a viewing portion 253, and seal anchor member 100. Asshown best in FIG. 10, a flexible, compliant ring 380 operably connectssurgical instruments 270. The ring 380 may be formed from a materialhaving shape memory properties, e.g., a nickel titanium alloy (nitinol)to bias the ring toward an expanded state.

In embodiments, the surgical instruments 270 and the ring 380 may bewelded or adhesively bound together. As shown in FIG. 9, bands 381 aredisposed about each surgical instrument and the bands 381 are coupled tothe ring 380. The ring 380 is transitionable between a first diameter Land a second diameter M. The ring may be formed, for example, from afoam, plastic, or rubber material having sufficient compliance totransition between diameters L, M. The ring 380 may be biased toward thelarger, second diameter M. The surgical instruments 270 are axiallytranslatable in a proximal direction “C” and in a distal direction “E”.When the surgical instruments 270 are drawn proximally (FIG. 11), thedecreased distance between the distal end of the ports 108 a-c means agreater force is needed to bend the surgical instruments 270 than isneeded when the surgical instruments 270 are extended distally (FIG.12). Translation of the surgical instruments 270 may effect asubstantially synchronized or coordinated repositioning of each of theend effectors 272 of the surgical instruments 270 relative to theviewing portion 253 of the viewing instrument 251. By knowing theinitial position, i.e., coordinates of the end effectors 272 of thesurgical instruments 270 relative to the viewing portion 253 of theviewing instrument 251, tracking of the coordinates of each of the endeffectors 272 is achievable.

The ring 380 applies a force to bend the surgical instruments 270 and toexpand the surgical instruments 270 apart. The force applied by the ring380 is counter to the biasing force of the surgical instruments 270 thatare biased toward a straight configuration. When the surgicalinstruments 270 are drawn proximally (FIG. 11), the decreased distancebetween the distal end of the ports 108 a-d means a greater force isneeded to bend the surgical instruments 270 than is needed when thesurgical instruments 270 are extended distally (FIG. 12) due to theincreased leverage distance (moment arm). Accordingly, distaltranslation of the surgical instruments 270 through the ports 108 a-ctriangulates the instruments with respect to the viewing instrument 251within the lumen 109 by bending the surgical instruments 270.Conversely, the proximal translation of the surgical instruments 270through the ports 108 a-c straightens the instruments 270, which due tothe relatively smaller diameter of the triangulation system 300 (in thefirst configuration shown in FIG. 11) facilitates insertion and removalof the triangulation device 300 from the opening “O” within tissue “T”(FIG. 1).

In yet another embodiment, a triangulation system 400 includes the sealanchor member 100, and a triangulation device 450A including one or moresurgical instruments 270 and a tube 450 adapted to receive the viewinginstrument 251 including a viewing portion 253 therethrough. The tube450 is placed within lumen 109 of the seal anchor member 100. Thesurgical instruments 270 are placed within ports 108 a-c of the sealanchor member 100.

As shown in FIG. 13, the tube 450 includes a balloon 452 at a distal endthereof. A source of inflation “S” provides a source of inflation fluid(e.g., CO₂ or saline) to the balloon 452 through conduit 7. In anon-inflated state (FIG. 13), the balloon 452 does not exert sufficientforce to overcome the biasing force of the surgical instruments 270. Asthe balloon inflates, the balloon 452 radially expands and exerts aforce against the surgical instruments 270 to overcome the biasing forceof the surgical instruments 270. As shown in FIG. 13, the surgicalinstruments 270 are inwardly biased such that the distal ends of thesurgical instruments are pressed against the surface of the balloon 452.Insertion of the triangulation system 400 within an opening “O” withintissue “T”.

In the inflated state, as shown in FIG. 14, the surgical instruments 270are bent and are outwardly splayed apart. By spreading the surgicalinstruments 270 apart, interference between the surgical instruments 270is inhibited.

In an embodiment, the internal bias and shape memory of the surgicalinstrument 270 facilitates placement of the end effectors 272 of thesurgical instrument before the viewing portion 253 of viewing instrument251 to facilitate visualization of the position of the end effectors272. The surgical instruments 270 may be affixed to the balloon 452, forexample, by an adhesive at fixation points 459. Furthermore, a band 457may be placed about the surgical instruments 270, as shown in FIGS. 13and 14. The band 457 may be placed at or near the distal end of thesurgical instruments 270 such that inflation of the balloon 452 resultsin the inward angling of the end effects 272 of surgical instruments270, thereby causing triangulation of the surgical instruments 270. Inan embodiment, a length of shrink wrap may be placed about the surgicalinstruments 270, the internal bias of which causes the surgicalinstruments 270 to be secured to the balloon 452.

The inflation of the balloon 452 results in a uniform and predictableinflation of the balloon 452 such that the shape and size of the balloon452 is known for a given volume of fluid, e.g., gas or liquid, withinthe balloon. Since the surgical instrument 270 is formed from acompliant material, the configuration of the surgical instrument 270corresponds to the configuration of the balloon 452. The positioning ofthe surgical instruments 270 depends on the inflation of the balloon 452and upon the positioning within the ports 108 a-c, i.e., axial positionof the surgical instrument 270 within each of the ports 108 a-c. Bytracking the axial position of the surgical instrument within the port108 a-c and the inflation level of the balloon 452, the position of theend effectors 272 of each surgical instrument 270 is determinable.

Although the illustrative embodiments of the present disclosure havebeen described herein with reference to the accompanying drawings, theabove description, disclosure, and figures should not be construed aslimiting, but merely as exemplifications of particular embodiments. Itis to be understood, therefore, that the disclosure is not limited tothose precise embodiments, and that various other changes andmodifications may be effected therein by one skilled in the art withoutdeparting from the scope or spirit of the disclosure.

What is claimed is:
 1. A surgical system comprising: a seal anchormember for positioning within a tissue tract accessing an underlyingbody cavity, the seal anchor member defining a longitudinal axis andincluding leading and trailing ends, an intermediate section disposedbetween the leading and trailing ends, and a plurality of portsextending between the leading and trailing ends; and a triangulationdevice including: a rotatable member received in a first port of theplurality of ports in a sealing relation; at least one surgicalinstrument configured to be received in a second port of the pluralityof ports in a sealing relation; and a linkage mechanism operablycoupling the at least one surgical instrument and the rotatable member,wherein rotation of the rotatable member transitions the at least onesurgical instrument between a first position in which the at least onesurgical instrument is substantially parallel to the longitudinal axisof the seal anchor member and a second position in which at least aportion of the at least one surgical instrument defines an acute anglewith respect to the longitudinal axis.
 2. The surgical system of claim1, wherein the linkage mechanism includes an arm member operablycoupling the at least one surgical instrument and the rotatable member.3. The surgical system of claim 2, wherein the linkage mechanism furtherincludes a collar threadably coupled with the rotatable member, wherebyrotation of the rotatable member causes movement of the collar along alength of the rotatable member.
 4. The surgical system of claim 3,wherein the linkage mechanism further includes a band positioned aboutthe at least one surgical instrument, the band pivotably connected tothe arm member.
 5. The surgical system of claim 4, wherein the armmember includes a first arm pivotably connected to the band and a secondarm pivotably connected to the collar, the first and second armspivotably coupled to each other.
 6. The surgical system of claim 1,wherein the at least one surgical instrument includes a weakened regionconfigured to bend upon application of a force thereto.
 7. The surgicalsystem of claim 1, wherein the at least one surgical instrument includesa hinge configured to bend upon application of a force thereto.
 8. Thesurgical system of claim 1, wherein the at least one surgical instrumentis formed of a compliant material.
 9. The surgical system of claim 1,wherein the plurality of ports extend longitudinally between the leadingand trailing ends of the seal anchor member.
 10. The surgical system ofclaim 1, wherein the triangulation device further includes a viewingportion operatively associated with the rotatable member.
 11. Thesurgical system of claim 1, wherein the at least one surgical instrumentincludes an end effector.
 12. A surgical system, comprising: a sealanchor member for positioning within a tissue tract accessing anunderlying body cavity, the seal anchor member including leading andtrailing ends, the seal anchor member defining a plurality of portsextending between the leading and trailing ends; and a triangulationdevice including: a rotatable member configured to be received through afirst port of the plurality of ports in a sealing relation; and at leastone surgical instrument received in a second port of the plurality ofports in a sealing relation, the at least one surgical instrumentoperatively coupled with the rotatable member, wherein rotation of therotatable member transitions the at least one surgical instrumentbetween a first position in which the at least one surgical instrumentis substantially parallel to a longitudinal axis defined by therotatable member and a second position in which at least a portion ofthe at least one surgical instrument defines an acute angle with respectto the longitudinal axis.
 13. The surgical system of claim 12, whereinthe triangulation device further includes a viewing portion operativelyassociated with the rotatable member.
 14. The surgical system of claim12, wherein triangulation device further includes a linkage mechanismoperably coupling the at least one surgical instrument and the rotatablemember, the linkage mechanism including an arm member operably couplingthe at least one surgical instrument and the viewing instrument.
 15. Thesurgical system of claim 14, wherein the linkage mechanism furtherincludes a collar threadably coupled with the rotatable member, wherebyrotation of the rotatable member causes movement of the collar along alength of the rotatable member.
 16. The surgical system of claim 15,wherein the linkage mechanism further includes a band positioned aboutthe at least one surgical instrument, the band pivotably connected tothe arm member.
 17. The surgical system of claim 16, wherein the armmember includes a first arm pivotably connected to the band and a secondarm pivotably connected to the collar, the first and second armspivotably coupled to each other.
 18. The surgical system of claim 12,wherein the at least one surgical instrument includes a hinge configuredto bend upon application of a force thereto.
 19. The surgical system ofclaim 12, wherein the at least one surgical instrument is formed of acompliant material.
 20. The surgical system of claim 12, wherein atleast one port of the plurality of ports extends longitudinally betweenthe leading and trailing ends of the seal anchor member.
 21. Thesurgical system of claim 12, wherein the at least one surgicalinstrument is disposed radially about the rotatable member.
 22. Thesurgical system of claim 12, wherein the at least one surgicalinstrument includes an end effector.
 23. The surgical system of claim12, wherein the at least one surgical instrument includes a weakenedregion configured to bend upon application of a force thereto.